Alterations of functional circuitry in aging brain and the impact of mutated APP expression

作者：Bearer Elaine L^*; Manifold Wheeler Brett C; Medina Christopher S; Gonzales Aaron G; Chaves Frances L; Jacobs Russell E

来源：Neurobiology of Aging, 2018, 70: 276-290.

DOI：10.1016/j.neurobiolaging.2018.06.018

• Amyloid precursor protein (APP)
• Fast axonal transport
• CA3 of the hippocampus
• Dentate gyrus
• Transgenic mice for Alzheimer's disease investigation
• Aging
• Manganese-enhanced magnetic resonance imaging (MEMRI)
• Cholinergic neurons
• Septal nuclei

Alzheimer's disease (AD) is a disease of aging that results in cognitive impairment, dementia, and death. Pathognomonic features of AD are amyloid plaques composed of proteolytic fragments of the amyloid precursor protein (APP) and neurofibrillary tangles composed of hyperphosphorylated tau protein. One type of familial AD occurs when mutant forms of APP are inherited. Both APP and tau are components of the microtubule-based axonal transport system, which prompts the hypothesis that axonal transport is disrupted in AD, and that such disruption impacts cognitive function. Transgenic mice expressing mutated forms of APP provide preclinical experimental systems to study AD. Here, we perform manganese-enhanced magnetic resonance imaging to study transport from hippocampus to forebrain in four cohorts of living mice: young and old wild-type and transgenic mice expressing a mutant APP with both Swedish and Indiana mutations (APPSwInd). We find that transport is decreased in normal aging and further altered in aged APPSwInd plaque-bearing mice. These findings support the hypothesis that transport deficits are a component of AD pathology and thus may contribute to cognitive deficits.

• 出版日期2018-10